Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Beaver-Visitec is recalling 214 ophthalmic procedure kits because the included Devon Light Gloves may have holes or slits that compromise sterility.
Dannmar is recalling MaxJax Portable Two-Post automatic car lift systems due to insufficient welding on lower carriage plates, which could cause the lift arms to snap and the vehicle to fall.
Roadtrek is recalling 335 model year 2014 motorhomes because electrical wiring under the front seats may damage, preventing the optional front thorax air bags from deploying in a crash.
Spartan Motors is recalling 2010-2015 Furion, Gladiator, and Metrostar emergency vehicles because the engine cooling fan may crack and detach, posing an injury risk to nearby individuals.
Texas Pack, Inc. is recalling 3,653 pounds of brown peeled shrimp in Texas due to a possible glass inclusion hazard.
Medtronic is recalling 18 Passive Planar Blunt Probes because they were manufactured with sharp tips instead of blunt tips. The devices are used in navigated surgery.
Byrd Cookie Company is recalling Vidalia Onion Biscuits because they contain undeclared anchovies, a common allergen.
Byrd Cookie Company is recalling Byrds Famous Cookies, Benne Bits, because the product contains undeclared anchovies.
Neuro Kinetics is recalling 140 I-Portal NOTC and VNG devices due to system malfunctions and unintended sudden movements at startup. No injuries have been reported.
Ford is recalling 2014-2015 Escape and Transit Connect vehicles because a software issue may cause the instrument panel to stop working, potentially hiding safety warnings.
Starcraft RV is recalling 50 model year 2014-2016 AR-ONE and Comet trailers because certification labels list the wrong tire size, which could lead to improper tire installation and increased crash risk.
General Motors is recalling specific Chevrolet Caprice and Pontiac G8 vehicles because seat belt cables may break, increasing injury risk in a crash.
Forest River is recalling 2015 Dynamax Rev vehicles because front head restraints may exceed safety limits, increasing injury risk in rear-end collisions.
Navistar is recalling 29,182 trucks and buses due to a wiring defect that could cause an electrical short and fire.
Champion is recalling 2013-2015 transit buses because seat belts may rub against metal frames and fray, failing federal safety standards.
Philips Medical Systems is recalling nine Ingenuity PET/MR Uninterruptible Power Supply (UPS) accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Reaction Nutrition is recalling Bio Armor Carno Pump Plus Electrolytes because shared equipment may cause unknown amounts of whey protein and soy contamination.
Flying Food Group is recalling Evolution Fresh brand Greek yogurt with berries and honey due to undeclared almonds. The product was distributed to stores in California.
Smith & Nephew is recalling 12 units of R3 Constrained Liners because the locking groove is oversized, which may prevent the locking ring from engaging properly.
Philips Medical Systems is recalling 36 Precedence 16 UPS accessory devices used in CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Philips is recalling 7 Gemini 16 PET/CT Uninterruptible Power Supply units worldwide due to risks of battery acid leakage, overheating, and fumes.
CooperSurgical is recalling five Ally Uterine Positioning System units because the design may expose users to injury to fingers or body parts.
Reaction Nutrition is recalling specific lots of RN BlueChip Creatine Monohydrate because shared equipment use may result in undeclared whey protein and soy.
AGFA Healthcare Corp. is recalling 233 mobile digital radiography x-ray systems due to a risk of sporadic unintended movements caused by electrostatic discharge.
Natural Creations is voluntarily recalling 399 bottles of New Zealand Colostrum dietary supplement because it contains an unidentified milk allergen.